Xunwei Jiang
Overview
Explore the profile of Xunwei Jiang including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
8
Citations
26
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Lin Q, Wang Z, Ding G, Li G, Chen L, Qiu Q, et al.
Front Immunol
. 2024 Nov;
15:1438640.
PMID: 39507528
Background: Kawasaki disease (KD) is an acute systemic vasculitis that can lead to acquired heart disease in children mostly from in developed countries. The previous research showed that B cells...
2.
Zhang L, Xu M, Yan Z, Han Y, Jiang X, Xiao T, et al.
BMC Med Genomics
. 2024 Oct;
17(1):250.
PMID: 39394151
Congenital long QT syndrome (LQTS) is a genetic heart disorder, which may lead to life-threatening arrhythmias, especially in children. Here, we reported two children who were initially misdiagnosed with epilepsy...
3.
Zheng J, Huang Z, Hou S, Jiang X, Zhang Y, Liu W, et al.
Front Pediatr
. 2022 Dec;
10:947963.
PMID: 36452351
Hypertrophic cardiomyopathy (HCM) is an autosomal dominant cardiomyopathy, which is one of the most common reasons for cardiac arrest in children or adolescents. It is characterized by ventricular hypertrophy (usually...
4.
Liu W, Liu T, Xiao T, Xie L, Hou C, Jiang X
Stem Cell Res
. 2022 Jun;
62:102811.
PMID: 35679758
TECRL, first reported in a Sudanese family with catecholaminergic polymorphic ventricular tachycardia (CPVT) in 2016. TECRL, is an endoplasmic reticulum (ER) protein preferentially expressed in the heart, playing a role...
5.
Hou C, Jiang X, Zhang H, Zheng J, Qiu Q, Zhang Y, et al.
Commun Biol
. 2022 May;
5(1):470.
PMID: 35577932
Sudden cardiac death (SCD) caused by ventricular arrhythmias is the leading cause of mortality of cardiovascular disease. Mutation in TECRL, an endoplasmic reticulum protein, was first reported in catecholaminergic polymorphic...
6.
Zong Y, Liu W, Hou C, Zhang H, Jiang X, Sun X, et al.
Transl Pediatr
. 2021 Sep;
10(8):2123-2130.
PMID: 34584883
Hereditary hemorrhagic telangiectasis (HHT) is an autosomal dominant vascular disease, and approximately 80% of all HHT cases are caused by gene mutation. In this report, we analyzed the case of...
7.
Xie L, Hou C, Jiang X, Zhao J, Li Y, Xiao T
Eur J Med Genet
. 2019 Feb;
62(7):103631.
PMID: 30790670
Catecholaminergic polymorphic ventricular tachycardia (CPVT) is one of the most common causes of sudden cardiac death (SCD) during childhood and in adolescence. Trans-2, 3-enoyl-CoA reductase-like (Tecrl) gene mutations (Arg196Gln and...
8.
Xie L, Li Y, Jiang X, Zhao J, Xiao T
BMC Pediatr
. 2019 Feb;
19(1):55.
PMID: 30744582
Background: Abernethy malformation is an extremely rare congenital malformation characterised by an extrahepatic portosystemic shunt. Children with Abernathy malformation can develop hepatopulmonary syndrome (HPS) with pulmonary arteriovenous fistulas (PAVF) or...